Infliximab for acute, not steroid-refractory ulcerative colitis:: a randomized pilot study

被引:97
作者
Ochsenkühn, T [1 ]
Sackmann, M [1 ]
Göke, B [1 ]
机构
[1] Univ Munich, Klinikum Grosshadern, Dept Med 2, D-81375 Munich, Germany
关键词
ulcerative colitis; infliximab; not steroid-refractory; randomized; prednisolone; controlled;
D O I
10.1097/00042737-200411000-00014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objective Therapeutic alternatives for patients with acute ulcerative colitis in whom steroids would usually be contraindicated are rare. The antibody to tumor necrosis factor alpha, infliximab, has shown to be effective in the treatment of steroid-refractory ulcerative colitis in pilot studies. We therefore evaluated whether infliximab can achieve remission in patients with acute ulcerative pancolitis who were not steroid-refractory. Methods and design Patients were eligible if they had acute disease with a modified Truelove and Witts activity score of more than 10 for at least 2 weeks and if they were currently not receiving immunomodulators or more than 10 mg/day prednisolone. Patients were randomly assigned to receive either three intravenous infusions of infliximab at 5 mg/kg (group A) or high-dose prednisolone (1.5 mg/kg body weight) daily for 2 weeks, followed by 1 mg/kg for 1 week, followed by a weekly reduction of 5 mg (group B). Therapy success was defined as clinical response in terms of a decrease of more than 5 points from the baseline score and to less than 10 points total after 3 weeks as well as after 13 weeks. Results Thirteen patients (seven women, six men) were randomized (six for group A and seven for group B). The median baseline activity scores were 13.5 (12-18) in group A and 14.0 (11-18) in group B. Five of six patients in group A and six of seven patients in group B showed therapy success after 3 weeks as well as after 13 weeks. Conclusions Infliximab could be effective in the treatment of acute moderate or severe ulcerative colitis. The obtained data call for larger controlled trials. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:1167 / 1171
页数:5
相关论文
共 38 条
[1]   CONTINUOUSLY INFUSED CYCLOSPORINE AT LOW-DOSE IS SUFFICIENT TO AVOID EMERGENCY COLECTOMY IN ACUTE ATTACKS OF ULCERATIVE-COLITIS WITHOUT THE NEED FOR HIGH-DOSE STEROIDS [J].
ACTIS, GC ;
OTTOBRELLI, A ;
PERA, A ;
BARLETTI, C ;
PONTI, V ;
PINNAPINTOR, M ;
VERME, G .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 1993, 17 (01) :10-13
[2]   Infliximab for treatment of steroid-refractory ulcerative colitis [J].
Actis, GC ;
Bruno, M ;
Pinna-Pintor, M ;
Rossini, FP ;
Rizzetto, M .
DIGESTIVE AND LIVER DISEASE, 2002, 34 (09) :631-634
[3]   Tumor necrosis factor α antibody (infliximab) therapy profoundly down-regulates the inflammation in Crohn's ileocolitis [J].
Baert, FJ ;
D'Haens, GR ;
Peeters, M ;
Hiele, MI ;
Schaible, TF ;
Shealy, D ;
Geboes, K ;
Rutgeerts, PJ .
GASTROENTEROLOGY, 1999, 116 (01) :22-28
[4]  
BLACKSTONE MO, 1984, ENDOSCOPIC INTERPRET
[5]   TUMOR-NECROSIS-FACTOR ALPHA-PRODUCING CELLS IN THE INTESTINAL-MUCOSA OF CHILDREN WITH INFLAMMATORY BOWEL-DISEASE [J].
BREESE, EJ ;
MICHIE, CA ;
NICHOLLS, SW ;
MURCH, SH ;
WILLIAMS, CB ;
DOMIZIO, P ;
WALKERSMITH, JA ;
MACDONALD, TT .
GASTROENTEROLOGY, 1994, 106 (06) :1455-1466
[6]   CYTOKINES (IMMUNOINFLAMMATORY HORMONES) AND THEIR NATURAL REGULATION IN INFLAMMATORY BOWEL-DISEASE (CROHNS-DISEASE AND ULCERATIVE-COLITIS) - A REVIEW [J].
BRYNSKOV, J ;
NIELSEN, OH ;
AHNFELTRONNE, I ;
BENDTZEN, K .
DIGESTIVE DISEASES, 1994, 12 (05) :290-304
[7]   Infliximab for patients with refractory ulcerative colitis [J].
Chey, WY .
INFLAMMATORY BOWEL DISEASES, 2001, 7 :S30-S33
[8]   Infliximab for refractory ulcerative colitis [J].
Chey, WY ;
Hussain, A ;
Ryan, C ;
Potter, GD ;
Shah, A .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2001, 96 (08) :2373-2381
[9]   Glucocorticoid-induced osteoporosis [J].
Clowes, JA ;
Peel, N ;
Eastell, R .
CURRENT OPINION IN RHEUMATOLOGY, 2001, 13 (04) :326-332
[10]   The safety profile of infliximab in patients with Crohn's disease: The Mayo Clinic experience in 500 patients [J].
Colombel, JF ;
Loftus, EV ;
Tremaine, WJ ;
Egan, LJ ;
Harmsen, WS ;
Schleck, CD ;
Zinsmeister, AR ;
Sandborn, WJ .
GASTROENTEROLOGY, 2004, 126 (01) :19-31